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- 抗原 See all SPG7 抗体
- SPG7 (Spastic Paraplegia 7 (SPG7))
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适用
- 人, 小鼠, 大鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This SPG7 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant fusion protein of human SPG7 (NP_003110.1).
- 亚型
- IgG
- Top Product
- Discover our top product SPG7 Primary Antibody
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anti-Spastic Paraplegia 7 (SPG7) (AA 300-573) antibody
SPG7 适用: 人, 小鼠 WB, IF, FACS 宿主: 小鼠 Monoclonal 1C12 unconjugated
anti-Spastic Paraplegia 7 (SPG7) (AA 300-573) antibodySPG7 适用: 人 WB, IF, FACS 宿主: 小鼠 Monoclonal 3H10 unconjugated
anti-Spastic Paraplegia 7 (SPG7) antibodySPG7 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Spastic Paraplegia 7 (SPG7) (AA 1-795) antibodySPG7 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Spastic Paraplegia 7 (SPG7) (AA 1-795) antibodySPG7 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Spastic Paraplegia 7 (SPG7) (AA 1-250) antibodySPG7 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Spastic Paraplegia 7 (SPG7) (AA 115-141) antibodySPG7 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB23654 unconjugated
anti-Spastic Paraplegia 7 (SPG7) (AA 114-141), (Middle Region) antibodySPG7 适用: 人 WB, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- WB 1:1000-1:2000
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 mg/mL
- 缓冲液
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- 抗原
- SPG7 (Spastic Paraplegia 7 (SPG7))
- 别名
- SPG7 (SPG7 产品)
- 别名
- CAR antibody, CMAR antibody, PGN antibody, SPG5C antibody, AI452278 antibody, AU015315 antibody, Cmar antibody, SPG7, paraplegin matrix AAA peptidase subunit antibody, SPG7 antibody, Spg7 antibody
- 背景
- This gene encodes a mitochondrial metalloprotease protein that is a member of the AAA family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. Mutations in this gene cause autosomal recessive spastic paraplegia 7. Two transcript variants encoding distinct isoforms have been identified.
- 分子量
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Observed_MW: 88kDa
Calculated_MW: 53kDa/88kDa
- 基因ID
- 6687
- UniProt
- Q9UQ90
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